NCT07124949

Brief Summary

The Chinese Migrant Population Health Cohort is a prospective, multi-center study jointly initiated by Professor Yong Ji, President of Harbin Medical University, and Academician Guoqiang Chen, President of Hainan Medical University, in collaboration with regional partners. It targets older adults (≥60 years) who engage in seasonal migration between cold (Heilongjiang) and tropical (Hainan) regions. The primary objective is to investigate cardiovascular and metabolic disease risks, underlying biological and environmental mechanisms, and effective preventive strategies in this unique population. Participants are recruited from both origin and destination sites and undergo standardized baseline assessments, including questionnaires, physical examinations, medical imaging, biospecimen collection (blood, stool, hair, nails), and environmental exposure monitoring. Longitudinal follow-up includes periodic reassessments, remote monitoring, and data linkage with hospital information systems to capture health outcomes. The study aims to: Define migration-related health risk profiles and disease phenotypes. Elucidate biological and environmental mechanisms influencing disease onset and progression. Develop AI-driven risk prediction models and evaluate targeted interventions through nested randomized controlled trials. Translate findings into clinical guidelines and scalable cross-regional health management models. This is the first cohort in China to systematically investigate the health impacts of seasonal migration in older adults. By integrating epidemiology, multi-omics, environmental data, and health policy translation, the study seeks to improve continuity of care, strengthen climate adaptation, and promote healthy ageing.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
26,000

participants targeted

Target at P75+ for all trials

Timeline
48mo left

Started Jul 2025

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress17%
Jul 2025Apr 2030

Study Start

First participant enrolled

July 23, 2025

Completed
19 days until next milestone

First Submitted

Initial submission to the registry

August 11, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 15, 2025

Completed
4.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2030

Last Updated

August 20, 2025

Status Verified

August 1, 2025

Enrollment Period

4.8 years

First QC Date

August 11, 2025

Last Update Submit

August 14, 2025

Conditions

Keywords

Cardiovascular DiseasesMetabolic DiseasesGeriatricsMigrationClimate ChangeHealth Promotion

Outcome Measures

Primary Outcomes (1)

  • Number of Participants Experiencing First Major Cardiovascular Event

    First occurrence of myocardial infarction, stroke (ischemic or hemorrhagic), or cardiovascular death, confirmed through hospital records, death registries, and adjudication committee review.

    Up to 5 years from baseline

Secondary Outcomes (5)

  • Number of Participants with New-Onset Metabolic Disorders

    Up to 5 years from baseline

  • Number of Deaths from Any Cause

    Up to 5 years from baseline

  • Changes in Cardiometabolic Risk Factors

    Baseline, 2 years, 4 years

  • Change in EQ-5D Quality of Life Score from Baseline

    Baseline, 2 years, 4 years

  • Change in Cognitive Function Score (MoCA) from Baseline

    Baseline, 2 years, 4 years

Other Outcomes (3)

  • Change in Carotid Intima-Media Thickness from Baseline

    Baseline and follow-up imaging

  • Change in Coronary Artery Calcium Score from Baseline

    Baseline and follow-up imaging

  • Change in Plasma Metabolite Levels from Baseline

    Baseline and follow-up biospecimen analyses

Study Arms (4)

Winter Migrant Group

No Intervention

Other: No intervention

Summer Migrant Group

No Intervention

Other: No intervention

Cold-Region Resident Group

no Intervention

Other: No intervention

Tropical-Region Resident Group

no Intervention

Other: No intervention

Interventions

no intervention

Cold-Region Resident GroupSummer Migrant GroupTropical-Region Resident GroupWinter Migrant Group

Eligibility Criteria

Age60 Years - 120 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study will enroll community-dwelling adults aged ≥60 years from Harbin (cold region) and Hainan (tropical region), China. Four groups will be included: 1. Winter Migrant Group: \~5,000 Harbin residents who habitually migrate to Hainan during the cold season for ≥2 months each time, with ≥2 consecutive years of such migration and plans to continue; 2. Summer Migrant Group: \~1,000 Hainan residents who habitually migrate to Harbin during the hot season for ≥2 months, with similar migration history and plans; 3. Cold-Region Resident Group: \~10,000 Harbin residents, including matched controls for migrant groups and randomly selected residents, with no \>2 months residence outside Harbin in the past 5 years; 4. Tropical-Region Resident Group: \~10,000 Hainan residents with similar matching criteria and residency requirements. All participants must be able to communicate, perform daily activities independently, consent to long-term follow-up, and provide biospecimens.

You may qualify if:

  • Permanent residents of Harbin or Hainan who will continue to reside in Harbin or Hainan for the next 5 years.
  • Baseline age ≥60 years, with basic communication and comprehension abilities.
  • No confirmed diagnosis of end-stage major organic diseases (e.g., advanced heart failure, advanced liver failure, advanced kidney failure, malignant tumors).
  • Able to perform activities of daily living independently and capable of completing questionnaires and physical examinations.
  • Willing to participate in the study, provide written informed consent, accept long-term follow-up, and provide biological specimens.

You may not qualify if:

  • Occurrence of life-threatening acute events (e.g., myocardial infarction, acute heart failure, stroke) within the past 30 days.
  • Currently receiving chronic treatment with antiviral drugs (e.g., for HIV) or antipsychotic medications.
  • Presence of moderate to severe cognitive impairment preventing survey completion or follow-up cooperation.
  • Current acute infectious diseases such as influenza or fever.
  • Simultaneous participation in other interventional clinical studies.
  • Refusal to sign informed consent or unwillingness to provide biological specimens.
  • Any other condition deemed unsuitable for study participation by the investigators based on overall assessment.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Harbin Medical University

Harbin, Heilongjiang, 150086,, China

RECRUITING

Related Publications (21)

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Biospecimen

Retention: SAMPLES WITH DNA

Whole blood (serum, plasma, buffy coat, and peripheral blood mononuclear cells), urine, stool, hair, and nail samples will be collected and stored. Blood samples will be processed for biochemical assays, DNA, RNA, and multi-omics analyses (including metabolomics, proteomics, and lipidomics). Urine and stool samples will be analyzed for metabolic, microbiome, and environmental exposure markers. Hair and nail samples will be used for long-term exposure assessment (e.g., heavy metals, stable isotopes). All biospecimens will be stored in a certified biobank at -80 °C for future research.

MeSH Terms

Conditions

Cardiovascular DiseasesMetabolic Diseases

Condition Hierarchy (Ancestors)

Nutritional and Metabolic Diseases

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Doctor

Study Record Dates

First Submitted

August 11, 2025

First Posted

August 15, 2025

Study Start

July 23, 2025

Primary Completion (Estimated)

April 30, 2030

Study Completion (Estimated)

April 30, 2030

Last Updated

August 20, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations